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Metro location and recognizable brand increase applicants, balanced by niche medical-device and OS-hardening skill needs.
High because medical-device OS hardening and regulatory compliance skills are industry-specific and less transferable.
High due to required medical-device regulatory experience, OS hardening expertise, and proven engineering leadership.
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Lead and develop a team responsible for system-level software components and automation focused on medical device platforms and IoT Windows/Linux OS hardening baselines.
Define the technical roadmap and oversee lifecycle management of Windows and Linux operating systems ensuring safe, secure, and compliant system behavior aligned with clinical, regulatory, and cybersecurity requirements.
Collaborate with global R&D, QA/RA, Cybersecurity, IT, and Service teams to implement cohesive end-to-end solutions compliant with medical device standards.
Bachelor’s or Master’s degree in Computer Science, Software Engineering, Electrical/Computer Engineering, or related field.
Significant experience in system-level software development (C/C++, low-level APIs, OS internals, hardware interaction) and/or scripting (PowerShell, Bash, Python) on Windows and/or Linux.
Proven experience leading or managing engineering teams in regulated or safety-critical domains, preferably medical devices.
Experience working under Quality Management Systems and with medical or comparable standards such as IEC 62304, ISO 13485, ISO 14971, IEC 81001-5-1, ISO 27001.
Experienced leader skilled in managing system software teams delivering complex OS hardening and automation solutions in a medical device context.
Strong technical expertise with Windows and Linux OS internals, deployment automation tools, and compliance with medical device regulations.
Ability to drive structured, risk-aware decisions prioritizing patient safety, regulatory compliance, and product quality in cross-functional environments.